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Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia
BACKGROUND: Several large, rare chromosomal copy number variants (CNVs) have recently been shown to increase risk for schizophrenia and other neuropsychiatric disorders including autism, ADHD, learning difficulties and epilepsy. AIMS: We wanted to examine the frequencies of these schizophrenia-assoc...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3315675/ https://ncbi.nlm.nih.gov/pubmed/22130109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.schres.2011.11.004 |
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